Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 143
... chromosome has been reported . Apparent duplication of supernumerary or abnormal chromosomes is frequently observed and seems to be a fundamental mechanism in the evolution of neoplastic processes [ 48 ] . When such an extra normal ...
... chromosome has been reported . Apparent duplication of supernumerary or abnormal chromosomes is frequently observed and seems to be a fundamental mechanism in the evolution of neoplastic processes [ 48 ] . When such an extra normal ...
Seite 144
figures , and polyploidy , as well as abnormal chromosomes strikingly similar to the marker chromosomes seen in tumor cells . Although the Ph1 chromosome has appar- ently not been obtained after irradiation of cells in vitro , recent ...
figures , and polyploidy , as well as abnormal chromosomes strikingly similar to the marker chromosomes seen in tumor cells . Although the Ph1 chromosome has appar- ently not been obtained after irradiation of cells in vitro , recent ...
Seite 428
... chromosome in early embryonic development , two XO lines may be formed in the affected individuals , one containing an active X - chromosome and the other an inactive X - chromosome . The cells containing the inactive X - chromosome may ...
... chromosome in early embryonic development , two XO lines may be formed in the affected individuals , one containing an active X - chromosome and the other an inactive X - chromosome . The cells containing the inactive X - chromosome may ...
Inhalt
Welcoming Address | 3 |
Remarks of the Secretary of the Permanent Committee for the International | 11 |
Diagnosis in medical genetics | 29 |
Urheberrecht | |
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abnormal acatalasia acatalatic acid Acta activity alleles Amer amino-acid amino-acid sequence analysis aneuploidy anomalies antibodies antigenic autosomal dominant autosomal recessive biochemical birth blood blood-group catalase cent child chromosome aberrations clinical colonies congenital consanguinity Cytogenetics defect deficiency Dept determined disaccharidases disease distribution duplication effects enzyme evolution factors female gamma globulin gene frequencies hemoglobin heredity is autosomal heterochromatin heterozygotes heterozygous Hospital Human Genetics inactivation individuals inheritance intestinal karyotype L-leut lactase Lancet leukemia linkage loci locus male malformations maltase marker marriage mating Medical mental metabolism Michigan Mongolism mosaic mutation normal observed pairs parents patients pattern pedigree peptide chains Ph¹ phenotype population possible Proc protein recombination records red cells selection sex chromatin sex-linked specific structure studies substance sucrase syndrome synthesis Table techniques tion tissue traits translocation trisomy University variable variation X-chromosome York